Composite electrolytes with binders

ABSTRACT

Functionalized polymeric binders for electrolyte and electrode compositions include a polymer having a polymer backbone and functional groups. In some embodiments, a polymer includes a non-polar polymer backbone and a functional group that is 0.1 to 5 wt % of the polymer. In some embodiments, a polymer includes a polar backbone and a functional group that is 0.1 to 50% weight percent of the polymer. Also described are composites for electrolyte separators and electrodes that include argyrodite ion conductors and polar polymers.

INCORPORATION BY REFERENCE

An Application Data Sheet is filed concurrently with this specificationas part of the present application. Each application that the presentapplication claims benefit of or priority to as identified in theconcurrently filed Application Data Sheet is incorporated by referenceherein in its entirety and for all purposes.

BACKGROUND

Solid-state electrolytes present various advantages over liquidelectrolytes for primary and secondary batteries. For example, inlithium ion secondary batteries, inorganic solid-state electrolytes maybe less flammable than conventional liquid organic electrolytes.Solid-state electrolytes can also faciliate use of a lithium metalelectrode by resisting dendrite formation. Solid-state electrolytes mayalso present advantages of high energy densities, good cyclingstabilities, and electrochemical stabilities over a range of conditions.However, there are various challenges in large scale commercializationof solid-state electrolytes. One challenge is maintaining contactbetween electrolyte and the electrodes. For example, while inorganicmaterials such as inorganic sulfide glasses and ceramics have high ionicconductivities (over 10-4 S/cm) at room temperature, they do not serveas efficient electrolytes due to poor adhesion to the electrode duringbattery cycling. Another challenge is that glass and ceramic solid-stateconductors are too brittle to be processed into dense, thin films on alarge scale. This can result in high bulk electrolyte resistance due tothe films being too thick, as well as dendrite formation, due to thepresence of voids that allow dendrite penetration. The mechanicalproperties of even relatively ductile sulfide glasses are not adequateto process the glasses into dense, thin films. Improving thesemechanical properties without sacrificing ionic conductivity is aparticular challenge, as techniques to improve adhesion, such as theaddition of a solid polymer binder, tend to reduce ionic conductivity.It is not uncommon to observe more than an order of magnitudeconductivity decrease with as little as 1 wt % of binder introduced.Solid-state polymer electrolyte systems may have improved mechanicalcharacteristics that faciliate adhesion and formation into thin films,but have low ionic conductivity at room temperature or poor mechanicalstrength.

Materials that have high ionic conductivities at room temperature andthat are sufficiently compliant to be processed into thin, dense filmswithout sacrificing ionic conductivity are needed for large scaleproduction and commercialization of solid-state batteries.

SUMMARY

One aspect of the disclosure relates to a composite including: inorganicionically conductive particles; and an organic phase including a polymerbinder, wherein the polymer binder includes a first polymer modifiedwith functional groups, the functional groups being between 0.1 and 5wt. % of the first polymer. In some embodiments, the first polymer is anon-polar polymer and the functional groups are polar groups. In someembodiments, the functional groups are selected from:

where R, R₁, R₂, R3 are independently for each occurrence selected from—CN, —H, —OH, Me⁺, —OMe⁺, optionally substituted aryl, optionallysubstituted alkoxy, optionally substituted alkyl, optionally substitutedalkenyl, and optionally substituted alkynyl; and X is independently foreach occurrence selected from —F , —Cl, —Br, and —I; and n is an integerfrom 1 to 10.

In some embodiments, the first polymer is one ofstyrene-butadiene-styrene (SBS), styrene-isoprene-styrene (SIS),styrene-ethylene/propylene-styrene (SEPS),styrene-ethylene/butylene-styrene (SEBS), styrene butadiene rubber(SBR), ethylene propylene diene monomer (EPDM) rubber, polybutadiene(PBD), polyethylene (PE), polypropylene (PP), and polystyrene (PS).

In some embodiments, the polymer binder includes SEBS modified withmaleic anhydride (SEBS-gMA). In some embodiments, the polymer binderincludes SEBS modified with furfurylamine (SEBS-gFA).

In some embodiments, the polymer binder includes a mixture of the firstpolymer modified with functional groups and an unmodified first polymer.

Another aspect of the disclosure relates to a slurry including: asolvent; a polymer binder dissolved in the solvent, the polymer binderincludes a first polymer modified with functional groups, the functionalgroups being between 0.1 and 5 wt. % of the first polymer; and ionicallyconductive sulfidic particles suspended in the solvent.

In some embodiments, the solvent has a polarity index of less than 3.5.In some embodiments, the solvent is halogenated and has a polarity indexof higher than 3.5. In some embodiments, the first polymer is anon-polar polymer and the functional groups are polar groups. In someembodiments, the functional groups are selected from:

where R, R₁, R₂, R₃ are independently for each occurrence selected from—CN, —H, —OH, Me⁺, —OMe⁺, optionally substituted aryl, optionallysubstituted alkoxy, optionally substituted alkyl, optionally substitutedalkenyl, and optionally substituted alkynyl; and X is independently foreach occurrence selected from —F, —Cl, —Br, and —I; and n is an integerfrom 1 to 10.

In some embodiments, the first polymer is one ofstyrene-butadiene-styrene (SBS), styrene-isoprene-styrene (SIS),styrene-ethylene/propylene-styrene (SEPS),styrene-ethylene/butylene-styrene (SEBS), styrene butadiene rubber(SBR), ethylene propylene diene monomer (EPDM) rubber, polybutadiene(PBD), polyethylene (PE), polypropylene (PP), and polystyrene (PS). Insome embodiments, the polymer binder includes SEBS modified with maleicanhydride (SEBS-gMA). In some embodiments, the polymer binder includesSEBS modified with furfurylamine (SEBS-gFA).

In some embodiments, the polymer binder includes a mixture of the firstpolymer modified with functional groups and an unmodified first polymer.

Another aspect of the disclosure relates to composite including:inorganic ionically conductive particles; and an organic phase includinga polymer binder, wherein the polymer binder includes a first polymermodified with functional groups, the functional groups being between 0.1and 50 wt. % of the first polymer. In some embodiments, the functionalgroups are between 5 and 50 wt. % of the first polymer.

In some embodiments, the first polymer unmodified is insoluble insolvents having polarity indexes below 4.5. In some such embodiments,the first polymer modified is soluble in the solvents having polarityindexes below 4.5. In some embodiments, the first polymer unmodified isinsoluble in solvents having polarity indexes below 3.5. In some suchembodiments, the first polymer modified is soluble in the solventshaving polarity indexes below 3.5. In some embodiments, the firstpolymer is polyvinylidene fluoride (PVDF). In some embodiments, thepolymer binder includes PVDF modified with styrene.

Another aspect of the disclosure relates to a slurry compositionincluding: a solvent; a polymer binder dissolved in the solvent, thepolymer binder includes a first polymer modified with functional groups,the functional groups being between 0.1 and 50 wt. % or 1 and 5 wt. % ofthe first polymer; and ionically conductive sulfidic particles suspendedin the solvent. In some embodiments, the first polymer unmodified isinsoluble in the solvent. In some such embodiments, the solvent has apolarity index below 4.5. In some such embodiments, the solvent has apolarity index below 3.5. In some embodiments, the first polymer ispolyvinylidene fluoride (PVDF). In some embodiments, the polymer binderincludes PVDF modified with styrene.

Another aspect of the disclosure relates to composite including:inorganic ionically conductive argyrodite-containing particles; and anorganic phase including a polar polymer binder.

In some embodiments, the composite has an ionic conductivity of at least0.2 mS·cm⁻¹ at 25° C., at least 0.25 mS·cm-1 at 25° C., or 0.3 mS·cm⁻¹at 25° C. In some such embodiments, the inorganic ionically conductiveargyrodite-containing particles are no more than 90wt %, 85wt %, or 80wt% of the composite. In some embodiments, the composite has an ionicconductivity of at least 0.6 mS·cm⁻¹ at 25° C., at least 0.6 mS·cm-1 at25° C., or 0.6 mS·cm⁻¹ at 25° C. In some such embodiments, the compositehas an elongation at break of at least 10%, 15%, or 20%.

In some embodiments, the polymer binder is poly(vinylacetate) or nitrilebutadiene rubber having up to 30% nitrile groups.

In some embodiments, the polymer binder ispoly(acrylonitrile-co-styrene-co-butadiene) (ABS),poly(ethylene-co-vinylacetate), poly(styrene-co-acrylonitrile) (SAN),poly(styrene-co-maleic anhydride), poly(meth)acrylates, poly(alkyeneglycols), poly(butadiene-co-acrylate), poly(butadiene-co-acrylicacid-co-acrylonitrile), Poly(ethylene-co-acrylates), polyethers,polyesters of dialkyl phthalates, or poly(vinyl chloride) (PVC).

In some embodiments, the polymer binder includes a first polymermodified with functional groups, the functional groups being between 0.1and 5 wt. % of the first polymer.

In some embodiments, the polymer binder includes a first polymermodified with functional groups, the functional groups being between 0.1and 50 wt. % of the first polymer. In some such embodiments, the firstpolymer unmodified is insoluble in solvents having polarity indexesbelow 3.5. In some embodiments, the first polymer modified is soluble inthe solvents having polarity indexes below 3.5.

In some embodiments, the argyrodite has the formulaLi_(7−x)PS_(6−x)X_(x) (X=Cl, Br, I, and 0<x<2). In some suchembodiments, X is greater than 1.

Another aspect of the disclosure relates to a composite including:inorganic ionically conductive argyrodite-containing particles; and anorganic phase including a polar polymer binder. In some embodiments, thepolar polymer binder is poly(vinylacetate) or nitrile butadiene rubberhaving up to 30% nitrile groups.

In some embodiments, is poly(acrylonitrile-co-styrene-co-butadiene)(ABS), poly(ethylene-co-vinylacetate), poly(styrene-co-acrylonitrile)(SAN), poly(styrene-co-maleic anhydride), poly(meth)acrylates,poly(alkyene glycols), poly(butadiene-co-acrylate),poly(butadiene-co-acrylic acid-co-acrylonitrile),poly(ethylene-co-acrylates), polyethers, polyesters of dialkylphthalates, or poly(vinyl chloride) (PVC).

In some embodiments, the polymer binder includes a first polymermodified with functional groups, the functional groups being between 0.1and 5 wt. % of the first polymer.

In some embodiments, the polymer binder includes a first polymermodified with functional groups, the functional groups being between 0.1and 50 wt. % of the first polymer.

In some such embodiments, the first polymer unmodified is insoluble insolvents having polarity indexes below 3.5. In some such embodiments,the first polymer modified is soluble in the solvents having polarityindexes below 3.5.

These and other aspects are described further below.

BRIEF DESCRIPTION OF DRAWINGS

FIGS. 1A-1C show schematic examples of cells according to variousembodiments.

FIG. 2 shows the crystal structure of cubic argyrodite Li₆PS₅Cl.

DESCRIPTION

Provided herein are ionically conductive composite electrolytes thathave an ionically-conductive inorganic phase and an organic phase. Thecomposites are single-ion conductors with good electrochemical stabilityand room temperature conductivities. The organic phase includes apolymeric binder that provides sufficient mechanical properties thatenable processing and incorporation in all-solid-state batteries. Thecomposite electrolytes can also provide high elasticity, bendability,and mechanical strength that may be needed for devices such as flexibleelectronics that are exposed to significant stresses during operation.

The term “number average molecular weight” or “Mn” in reference to aparticular component (e.g., a high molecular weight polymer binder) of asolid-state composition refers to the statistical average molecularweight of all molecules of the component expressed in units of g/mol.The number average molecular weight may be determined by techniquesknown in the art such as, for example, gel permeation chromatography(wherein Mn can be calculated based on known standards based on anonline detection system such as a refractive index, ultraviolet, orother detector), viscometry, mass spectrometry, or colligative methods(e.g., vapor pressure osmometry, end-group determination, or protonNMR). The number average molecular weight is defined by the equationbelow,

$M_{n} = \frac{\sum{N_{i}M_{i}}}{\sum N_{i}}$

wherein Mi is the molecular weight of a molecule and Ni is the number ofmolecules of that molecular weight. In the description below, referencesto molecular weights of particular polymers refer to number averagemolecular weight.

The term “alkyl” as used herein alone or as part of another group,refers to a straight or branched chain hydrocarbon containing any numberof carbon atoms and that include no double or triple bonds in the mainchain. “Lower alkyl” as used herein, is a subset of alkyl and refers toa straight or branched chain hydrocarbon group containing from 1 to 6carbon atoms. The terms “alkyl” and “lower alkyl” include bothsubstituted and unsubstituted alkyl or lower alkyl unless otherwiseindicated. Examples of lower alkyl include methyl, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, tert-butyl, and the like.

The alkyl group can also be substituted or unsubstituted. For example,the alkyl group can be substituted with one, two, three or, in the caseof alkyl groups of two carbons or more, four substituents independentlyselected from the group consisting of: (1) C¹⁻⁶ alkoxy (e.g., —O-Ak,wherein Ak is optionally substituted C¹⁻⁶ alkyl); (2) C¹⁻⁶ alkylsulfinyl(e.g., —S(O)-Ak, wherein Ak is optionally substituted C₁₋₆ alkyl); (3)C₁₋₆ alkylsulfonyl (e.g., —SO₂-Ak, wherein Ak is optionally substitutedC¹⁻⁶ alkyl); (4) amino (e.g., —NR^(N1)R^(N2), where each of R^(N1) andR^(N2) is, independently, H or optionally substituted alkyl, or R^(N1)and R^(N2), taken together with the nitrogen atom to which each areattached, form a heterocyclyl group); (5) aryl; (6) arylalkoxy (e.g.,—O-L-Ar, wherein L is a bivalent form of optionally substituted alkyland Ar is optionally substituted aryl); (7) aryloyl (e.g., —C(O)—Ar,wherein Ar is optionally substituted aryl); (8) azido (e.g., —N═N—); (9)cyano (e.g., —CN); (10) carboxyaldehyde (e.g., —C(O)H); (11) C₃₋₈cycloalkyl (e.g., a monovalent saturated or unsaturated non-aromaticcyclic C₃₋₈ hydrocarbon group); (12) halo (e.g., F, Cl, Br, or I); (13)heterocyclyl (e.g., a 5-, 6- or 7-membered ring, unless otherwisespecified, containing one, two, three, or four non-carbon heteroatoms,such as nitrogen, oxygen, phosphorous, sulfur, or halo); (14)heterocyclyloxy (e.g., —O-Het, wherein Het is heterocyclyl, as describedherein); (15) heterocyclyloyl (e.g., —C(O)-Het, wherein Het isheterocyclyl, as described herein); (16) hydroxyl (e.g., —OH); (17)N-protected amino; (18) nitro (e.g., —NO₂); (19) oxo (e.g., ═O); (20)C₃₋₈ spirocyclyl (e.g., an alkylene or heteroalkylene diradical, bothends of which are bonded to the same carbon atom of the parent group);(21) C₁₋₆ thioalkoxy (e.g., —S-Ak, wherein Ak is optionally substitutedC₁₋₆ alkyl); (22) thiol (e.g., —SH); (23) —CO₂R^(A), where R^(A) isselected from the group consisting of (a) hydrogen, (b) C₁₋₆ alkyl, (c)C₄₋₁₈ aryl, and (d) (C₄₋₁₈ aryl) C₁₋₆ alkyl (e.g., -L-Ar, wherein L is abivalent form of optionally substituted alkyl group and Ar is optionallysubstituted aryl); (24) —C(O)NR^(B)R^(c), where each of RB and Rc is,independently, selected from the group consisting of (a) hydrogen, (b)C₁₋₆ alkyl, (c) C₄₋₁₈ aryl, and (d) (C₄₋₁₈ aryl) C₁₋₆ alkyl (e.g.,-L-Ar, wherein L is a bivalent form of optionally substituted alkylgroup and Ar is optionally substituted aryl); (25) —SO₂R^(D), whereR^(D) is selected from the group consisting of (a) C₁₋₆ alkyl, (b) C₄₋₁₈aryl, and (c) (C₄₋₁₈ aryl) C₁₋₆ alkyl (e.g., -L-Ar, wherein L is abivalent form of optionally substituted alkyl group and Ar is optionallysubstituted aryl); (26) —SO₂NR^(E)R^(F), where each of R^(E) and R^(F)is, independently, selected from the group consisting of (a) hydrogen,(b) C₁₋₆ alkyl, (c) C₄₋₁₈ aryl, and (d) (C₄₋₁₈ aryl) C₁₋₆ alkyl (e.g.,-L-Ar, wherein L is a bivalent form of optionally substituted alkylgroup and Ar is optionally substituted aryl); and (27) —NR^(G)R^(H),where each of R^(G) and R^(H) is, independently, selected from the groupconsisting of (a) hydrogen, (b) an N-protecting group, (c) C₁₋₆ alkyl,(d) C₂₋₆ alkenyl (e.g., optionally substituted alkyl having one or moredouble bonds), (e) C₂₋₆ alkynyl (e.g., optionally substituted alkylhaving one or more triple bonds), (f) C₄₋₁₈ aryl, (g) (C₄₋₁₈ aryl) C₁₋₆alkyl (e.g., L-Ar, wherein L is a bivalent form of optionallysubstituted alkyl group and Ar is optionally substituted aryl), (h) C₃₋₈cycloalkyl, and (i) (C₃₋₈ cycloalkyl) C₁₋₆ alkyl (e.g., -L-Cy, wherein Lis a bivalent form of optionally substituted alkyl group and Cy isoptionally substituted cycloalkyl, as described herein), wherein in oneembodiment no two groups are bound to the nitrogen atom through acarbonyl group or a sulfonyl group. The alkyl group can be a primary,secondary, or tertiary alkyl group substituted with one or moresubstituents (e.g., one or more halo or alkoxy). In some embodiments,the unsubstituted alkyl group is a C₁₋₃, C₁₋₆, C₁₋₁₂, C₁₋₁₆, C₁₋₁₈,C₁₋₂₀, or C₁₋₂₄ alkyl group.

By “alkenyl” is meant an optionally substituted C₂₋₂₄ alkyl group havingone or more double bonds. The alkenyl group can be cyclic (e.g., C₃₋₂₄cycloalkenyl) or acyclic. The alkenyl group can also be substituted orunsubstituted. For example, the alkenyl group can be substituted withone or more substitution groups, as described herein for alkyl. In someembodiments, the unsubstituted alkenyl group is a C₂₋₆, C₂₋₁₂, C₂₋₁₆,C₂₋₁₈, C₂₋₂₀, or C₂₋₂₄ alkenyl group.

By “alkynyl” is meant an optionally substituted C₂₋₂₄ alkyl group havingone or more triple bonds. The alkynyl group can be cyclic or acyclic andis exemplified by ethynyl, 1-propynyl, and the like. The alkynyl groupcan also be substituted or unsubstituted. For example, the alkynyl groupcan be substituted with one or more substitution groups, as describedherein for alkyl. In some embodiments, the unsubstituted alkynyl groupis a C₂₋₆, C₂₋₁₂, C₂₋₁₆, C₂₋₁₈, C₂₋₂₀, or C₂₋₂₄ alkynyl group.

By “alkoxy” is meant —OR, where R is an optionally substituted alkylgroup, as described herein. Exemplary alkoxy groups include methoxy,ethoxy, butoxy, trihaloalkoxy, such as trifluoromethoxy, etc. The alkoxygroup can be substituted or unsubstituted. For example, the alkoxy groupcan be substituted with one or more substitution groups, as describedherein for alkyl. Exemplary unsubstituted alkoxy groups include C₁₋₃,C₁₋₆, C₁₋₁₂, C₁₋₁₆, C₁₋₁₈, C₁₋₂₀, or C₁₋₂₄ alkoxy groups.

The term “aryl” as used herein refers to groups that include monocyclicand bicyclic aromatic groups. Examples include phenyl, benzyl,anthracenyl, anthryl, benzocyclobutenyl, benzocyclooctenyl, biphenylyl,chrysenyl, dihydroindenyl, fluoranthenyl, indacenyl, indenyl, naphthyl,phenanthryl, phenoxybenzyl, picenyl, pyrenyl, terphenyl, and the like,including fused benzo-C₄₋₈ cycloalkyl radicals (e.g., as defined herein)such as, for instance, indanyl, tetrahydronaphthyl, fluorenyl, and thelike. The term aryl also includes heteroaryl, which is defined as agroup that contains an aromatic group that has at least one heteroatomincorporated within the ring of the aromatic group. Examples ofheteroatoms include, but are not limited to, nitrogen, oxygen, sulfur,and phosphorus. Likewise, the term non-heteroaryl, which is alsoincluded in the term aryl, defines a group that contains an aromaticgroup that does not contain a heteroatom. The aryl group can besubstituted or unsubstituted. The aryl group can be substituted withone, two, three, four, or five substituents, such as those describedherein for alkyl. In particular embodiments, an unsubstituted aryl groupis a C₄₋₁₈, C₄₋₁₄, C₄₋₁₂, C₄₋₁₀, C₆₋₁₈, C₆₋₁₄, C₆₋₁₂, or C₆₋₁₀ arylgroup.

By “heterocyclyl” is meant a 3-, 4-, 5-, 6- or 7-membered ring (e.g., a5-, 6- or 7-membered ring), unless otherwise specified, containing one,two, three, or four non-carbon heteroatoms (e.g., independently selectedfrom the group consisting of nitrogen, oxygen, phosphorous, sulfur,selenium, or halo). The 3-membered ring has zero to one double bonds,the 4- and 5-membered ring has zero to two double bonds, and the 6- and7-membered rings have zero to three double bonds. The term“heterocyclyl” also includes bicyclic, tricyclic and tetracyclic groupsin which any of the above heterocyclic rings is fused to one, two, orthree rings independently selected from the group consisting of an arylring, a cyclohexane ring, a cyclohexene ring, a cyclopentane ring, acyclopentene ring, and another monocyclic heterocyclic ring, such asindolyl, quinolyl, isoquinolyl, tetrahydroquinolyl, benzofuryl,benzothienyl and the like. Heterocyclics include acridinyl, adenyl,alloxazinyl, azaadamantanyl, azabenzimidazolyl, azabicyclononyl,azacycloheptyl, azacyclooctyl, azacyclononyl, azahypoxanthinyl,azaindazolyl, azaindolyl, azecinyl, azepanyl, azepinyl, azetidinyl,azetyl, aziridinyl, azirinyl, azocanyl, azocinyl, azonanyl,benzimidazolyl, benzisothiazolyl, benzisoxazolyl, benzodiazepinyl,benzodiazocinyl, benzodihydrofuryl, benzodioxepinyl, benzodioxinyl,benzodioxanyl, benzodioxocinyl, benzodioxolyl, benzodithiepinyl,benzodithiinyl, benzodioxocinyl, benzofuranyl, benzophenazinyl,benzopyranonyl, benzopyranyl, benzopyrenyl, benzopyronyl,benzoquinolinyl, benzoquinolizinyl, benzothiadiazepinyl,benzothiadiazolyl, benzothiazepinyl, benzothiazocinyl, benzothiazolyl,benzothienyl, benzothiophenyl, benzothiazinonyl, benzothiazinyl,benzothiopyranyl, benzothiopyronyl, benzotriazepinyl, benzotriazinonyl,benzotriazinyl, benzotriazolyl, benzoxathiinyl, benzotrioxepinyl,benzoxadiazepinyl, benzoxathiazepinyl, benzoxathiepinyl,benzoxathiocinyl, benzoxazepinyl, benzoxazinyl, benzoxazocinyl,benzoxazolinonyl, benzoxazolinyl, benzoxazolyl, benzylsultamylbenzylsultimyl, bipyrazinyl, bipyridinyl, carbazolyl (e.g.,4H-carbazolyl), carbolinyl (e.g., β-carbolinyl), chromanonyl, chromanyl,chromenyl, cinnolinyl, coumarinyl, cytdinyl, cytosinyl,decahydroisoquinolinyl, decahydroquinolinyl, diazabicyclooctyl,diazetyl, diaziridinethionyl, diaziridinonyl, diaziridinyl, diazirinyl,dibenzisoquinolinyl, dibenzoacridinyl, dibenzocarbazolyl,dibenzofuranyl, dibenzophenazinyl, dibenzopyranonyl, dibenzopyronyl(xanthonyl), dibenzoquinoxalinyl, dibenzothiazepinyl, dibenzothiepinyl,dibenzothiophenyl, dibenzoxepinyl, dihydroazepinyl, dihydroazetyl,dihydrofuranyl, dihydrofuryl, dihydroisoquinolinyl, dihydropyranyl,dihydropyridinyl, dihydroypyridyl, dihydroquinolinyl, dihydrothienyl,dihydroindolyl, dioxanyl, dioxazinyl, dioxindolyl, dioxiranyl, dioxenyl,dioxinyl, dioxobenzofuranyl, dioxolyl, dioxotetrahydrofuranyl,dioxothiomorpholinyl, dithianyl, dithiazolyl, dithienyl, dithiinyl,furanyl, furazanyl, furoyl, furyl, guaninyl, homopiperazinyl,homopiperidinyl, hypoxanthinyl, hydantoinyl, imidazolidinyl,imidazolinyl, imidazolyl, indazolyl (e.g., 1H-indazolyl), indolenyl,indolinyl, indolizinyl, indolyl (e.g., 1H-indolyl or 3H-indolyl),isatinyl, isatyl, isobenzofuranyl, isochromanyl, isochromenyl,isoindazoyl, isoindolinyl, isoindolyl, isopyrazolonyl, isopyrazolyl,isoxazolidiniyl, isoxazolyl, isoquinolinyl, isoquinolinyl,isothiazolidinyl, isothiazolyl, morpholinyl, naphthindazolyl,naphthindolyl, naphthiridinyl, naphthopyranyl, naphthothiazolyl,naphthothioxolyl, naphthotriazolyl, naphthoxindolyl, naphthyridinyl,octahydroisoquinolinyl, oxabicycloheptyl, oxauracil, oxadiazolyl,oxazinyl, oxaziridinyl, oxazolidinyl, oxazolidonyl, oxazolinyl,oxazolonyl, oxazolyl, oxepanyl, oxetanonyl, oxetanyl, oxetyl, oxtenayl,oxindolyl, oxiranyl, oxobenzoisothiazolyl, oxochromenyl,oxoisoquinolinyl, oxoquinolinyl, oxothiolanyl, phenanthridinyl,phenanthrolinyl, phenazinyl, phenothiazinyl, phenothienyl(benzothiofuranyl), phenoxathiinyl, phenoxazinyl, phthalazinyl,phthalazonyl, phthalidyl, phthalimidinyl, piperazinyl, piperidinyl,piperidonyl (e.g., 4-piperidonyl), pteridinyl, purinyl, pyranyl,pyrazinyl, pyrazolidinyl, pyrazolinyl, pyrazolopyrimidinyl, pyrazolyl,pyridazinyl, pyridinyl, pyridopyrazinyl, pyridopyrimidinyl, pyridyl,pyrimidinyl, pyrimidyl, pyronyl, pyrrolidinyl, pyrrolidonyl (e.g.,2-pyrrolidonyl), pyrrolinyl, pyrrolizidinyl, pyrrolyl (e.g.,2H-pyrrolyl), pyrylium, quinazolinyl, quinolinyl, quinolizinyl (e.g.,4H-quinolizinyl), quinoxalinyl, quinuclidinyl, selenazinyl, selenazolyl,selenophenyl, succinimidyl, sulfolanyl, tetrahydrofuranyl,tetrahydrofuryl, tetrahydroisoqui nolinyl, tetrahydroisoquinolyl,tetrahydropyridinyl, tetrahydropyridyl (piperidyl), tetrahydropyranyl,tetrahydropyronyl, tetrahydroquinolinyl, tetrahydroquinolyl,tetrahydrothienyl, tetrahydrothiophenyl, tetrazinyl, tetrazolyl,thiadiazinyl (e.g., 6H-1,2,5-thiadiazinyl or 2H,6H-1,5,2-dithiazinyl),thiadiazolyl, thianthrenyl, thianyl, thianaphthenyl, thiazepinyl,thiazinyl, thiazolidinedionyl, thiazolidinyl, thiazolyl, thienyl,thiepanyl, thiepinyl, thietanyl, thietyl, thiiranyl, thiocanyl,thiochromanonyl, thiochromanyl, thiochromenyl, thiodiazinyl,thiodiazolyl, thioindoxyl, thiomorpholinyl, thiophenyl, thiopyranyl,thiopyronyl, thiotriazolyl, thiourazolyl, thioxanyl, thioxolyl,thymidinyl, thyminyl, triazinyl, triazolyl, trithianyl, urazinyl,urazolyl, uretidinyl, uretinyl, uricyl, uridinyl, xanthenyl, xanthinyl,xanthionyl, and the like, as well as modified forms thereof (e.g.,including one or more oxo and/or amino) and salts thereof. Theheterocyclyl group can be substituted or unsubstituted. For example, theheterocyclyl group can be substituted with one or more substitutiongroups, as described herein for alkyl.

Introduction

lonically conductive composite electrolytes that have anionically-conductive inorganic phase and a non-ionically-conductiveorganic phase address various challenges of fabricating and using solidstate electrolytes. Certain embodiments of the composite electrolyteshave relative high polymer loadings (e.g., about 50 vol. %). This canpermit use in flexible electronics, and provide good mechanicalproperties.

Most state-of-the-art composite electrolytes with high organic contentrely on ionically conductive polymer matrix rather than inorganicconductors. Typical polymer electrolytes are prepared by dissolvinginorganic salt in a polymer matrix, which produces non-single-ionconductors with relatively low ionic conductivities and transferencenumbers, and that require elevated temperatures for proper operation. Inaddition, they tend to have poor oxidative stability and decomposeduring cell operation, leading to inefficiencies in cycling performanceand lowered cell life-time. However, mechanical properties of polymersenable easy processing, good interfacial contact with electrodes andflexibility for proper handling and operation of solid-state batteries.Polymer electrolytes can be prepared as composites, with eitherionically-conductive or non-conductive inorganic fillers, that canimprove both their mechanical and electrochemical properties.Nonetheless, even with addition of inorganic particles, polymerelectrolytes still suffer from stability issues and non-single-iontransfer properties.

Provided herein are ionically conductive composite electrolytes thathave an ionically-conductive inorganic phase and an organic phase. Insome embodiments, the composites are single-ion conductors with goodelectrochemical stability and room temperature conductivities. Theorganic phase includes a polymeric binder that provides sufficientmechanical properties that enable processing and incorporation inall-solid-state batteries. The composite electrolytes can also providehigh elasticity, bendability, and mechanical strength that may be neededfor devices such as flexible electronics that are exposed to significantstresses during operation.

Organic Phase

The organic polymer phase may include one or more polymers and ischemically compatible with the inorganic ion conductive particles. Insome embodiments, the organic phase has substantially no ionicconductivity, and is referred to as “non-ionically conductive.”Non-ionically conductive polymers are described herein have ionicconductivities of less than 0.0001 S/cm.

According to various embodiments, the organic phase may include apolymeric binder that is polar or non-polar. There are different typesof physical forces that occur intramolecularly. Such forces vary instrength and are largely based on structures of interacting molecules.The weakest forces are known as dispersion forces (also referred to asLondon dispersion forces and van der Waals forces), which exist in allatoms and molecules. Such forces are caused by temporary dipoles, whichoccur due to uneven distribution of electrons in atoms/molecules, whichinduce opposite dipoles in neighboring molecules/atom. The formation oftemporary dipoles induces partial positive and negative charges that arethe source of positive attractions. Such attractions increase with thesize of the electron cloud, molar mass and surface are of particles.These are the only type of interactions found in nonpolar molecules andnoble gasses. Dipole-dipole Forces occur by permanent dipoles in polarmolecules, where molecules arrange in such way that partial positivecharges of one particle is next to the negative one on the neighboringmolecule. The forces are stronger than London dispersion forces andincrease with increasing electronegativity difference between atomsforming dipoles. That attraction also increases with decreasing size ofattracted molecule as the distance between attracting moleculesdecreases. Hydrogen bonding is a specific, strong type of dipole-dipoleinteractions that occurs between molecules that contain hydrogen atomsattached directly to small, highly electronegative atoms such asnitrogen (N), oxygen (O), or fluorine (F). In such cases, permanentpartial positive and negative charges are formed on hydrogen andelectronegative atoms respectively. Such permanent partial charges leadto even stronger attraction forces than in case of dipole-dipole forces.Ion-dipole Forces are caused by either ion or the charge attracted tothe opposite permanent dipoles occurring in polar molecules in a waythat ion is surrounded by molecules with the dipole with oppositecharge. These forces, for instance, are responsible for dissolution ofsalts, such as in electrolytes in lithium-ion batteries or in metal ioncomplexes with organic ligands.

In the description herein, a non-polar binder is one that materials thatin their pure form interact intramolecularly through weak dispersionforces. Such materials have little to no contribution from other,stronger interactions, such as dipole-dipole, or hydrogen bonding thatcan influence composite electrolyte. Examples includestyrene-ethylene-butylene-styrene (SEBS), styrene-butadiene-styrene(SBS), polystyrene (PSt), styrene-isoprene-styrene (SIS), andpolyethylene. Such materials show poor affinity and weak interactionswith inorganic materials, such as solid-state lithium ion conductors orlithium salts. In some instances, the presence of a polar group can betolerated at low concentrations, as long as the contribution of strongerforces is negligible. For example, a binder that has less than 2 wt % orless than 0.5 wt % polar groups may still be non-polar if thecontribution of the stronger forces is negligible. Other polymericbinders are polar. In yet other embodiments, a non-polar binder is orincludes a hydrocarbon (e.g., includes only carbon and hydrogen atoms).A polar binder has a noticeable effect of stronger attraction forces oncomposite electrolyte properties. These properties include, but are notlimited to, tensile strength, modulus, elongation at break, ionicconductivity, and particle dispersibility. The level of polarity can befrom very low to very high. Examples of lower polarity binders includeSEBS modified with grafted maleic anhydride or SBS modified withcarboxylic acid. Polarity depends on the nature of polar groups as wellas their weight fraction. In some embodiments, this may be as low as 0.1wt %. In some embodiments, it is more than 0.5 wt % , for example 1-5 wt%. More polar binders can include polymers with greater than 5% ofgrafted polar groups. Examples of very polar polymers includepoly(vinylacetate) and poly(methylmethacrylate) PMMA. In yet otherembodiments, a polar binder is or includes a hydrocarbon having one ormore non-carbon heteroatoms (e.g., nitrogen, oxygen, sulfur, silicon,etc.). Such heteroatoms can be provided by way of grafted functionalgroups, as described herein.

In some embodiments, the organic phase includes a polymer binder, arelatively high molecular weight polymer or mixture of different highmolecular weight polymers. A polymer binder has a molecular weight of atleast 30 kg/mol, and may be at least 50 kg/mol, or 100 kg/mol. Themolecular weight distribution can be monomodal, bimodal and multimodal.

In some embodiments, the polymer binder has a non-polar backbone.Examples of non-polar polymer binders include polymers or copolymersincluding styrene, butadiene, isoprene, ethylene, and butylene. Styrenicblock copolymers including polystyrene blocks and rubber blocks may beused, with examples of rubber blocks including polybutadiene (PBD) andpolyisoprene (PI). The rubber blocks may or may be hydrogenated.Specific examples of polymer binders are styrene ethylene butylenestyrene (SEBS), styrene-butadiene-styrene (SBS),styrene-isoprene-styrene (SIS), styrene-butadiene rubber (SBR),polystyrene (PSt), PBD, polyethylene (PE), and PI. Non-polar polymers donot coat the inorganic particles, which can lead to reducedconductivity.

The main chain or backbone of the polymeric components of the organicphase do not interact strongly with the inorganic phase. Examples ofbackbones include saturated or unsaturated polyalkyls, polyaromatics,and polysiloxanes. Examples of backbones that may interact too stronglywith the inorganic phase include those with strong electron donatinggroups such as polyalcohols, polyacids, polyesters, polyethers,polyamines, and polyamides. It is understood that molecules that haveother moieties that decrease the binding strength of oxygen or othernucleophile groups may be used. For example, the perfluorinatedcharacter of a perfluorinated polyether (PFPE) backbone delocalizes theelectron density of the ether oxygens and allows them to be used incertain embodiments.

In some embodiments, hydrophobic block copolymers having both plasticand elastic copolymer segments are used. Examples include styrenic blockcopolymers such as SEBS, SBS, SIS, styrene-isoprene/butadiene-styrene(SIBS), styrene-ethylene/propylene (SEP),styrene-ethylene/propylene-styrene (SEPS), and isoprene rubber (IR).

In embodiments in which the binder is a copolymer, the constituentpolymers may be distributed in any appropriate manner such that thebinder can be a block copolymer, a random copolymer, a statisticalcopolymer, a graft copolymer, etc. The polymer backbone may be linear ornon-linear with examples including branched, star, comb, and bottlebrushpolymers. Further, transitions between constituent polymers of acopolymer can be sharp, tapered, or random.

In some embodiments, the organic phase is substantially non-ionicallyconductive, with examples of non-ionically conductive polymers includingPDMS, PBD, and the other polymers described above. Unlike ionicallyconductive polymers such as polyethylene oxide (PEO), polypropyleneoxide (PPO), polyacrylonitrile (PAN), poly(methyl methacrylate) (PMMA),which are ionically conductive because they dissolve or dissociate saltssuch as Lil, non-ionically conductive polymers are not ionicallyconductive even in the presence of a salt. This is because withoutdissolving a salt, there are no mobile ions to conduct. In someembodiments, one of these or another ionically conductive polymer may beused. PFPE's, referred to above, and described in Compliantglass-polymer hybrid single ion-conducting electrolytes for lithium ionbatteries, PNAS, 52-57, vol. 113, no. 1 (2016), incorporated byreference herein, are ionically conductive, being single ion-conductorsfor lithium and may be used in some embodiments.

In some embodiments, the organic phase may included cross-linking. Insome embodiments, the organic phase is a cross-linked polymer network.Cross-linked polymer networks can be cross-linked in-situ, i.e., afterthe inorganic particles are mixed with polymer or polymer precursors toform a composite. In-situ polymerization, including in-situcross-linking, of polymers is described in U.S. Pat. No. 10,079,404,incorporated by reference herein.

Polar Polymeric Binders

Polar polymeric binders that are used in other battery applications,such as carboxymethyl cellulose (CMC), polyethylene oxide (PEO), andpolyvinylidene fluoride (PVDF), lead to composites having poor ionicconductivity if mixed with inorganic conductors. This is because thepolymers can bind strongly to surface of inorganic particles, forming adense, insulating coating that prevents direct contact with neighboringparticles. Even as low as 1-5 wt. % of such polymers can insulateparticles and block lithium-ion pathways across the composite, leadingto very resistive materials.

In some embodiments, the polymer binder is a thermoplastic elastomersuch as SEBS, SBS, or SIS. The non-polarity and hydrophobic character ofsuch binders allow for high retention of initial conductivity of pureinorganic conductors. In composite materials, including electrolyteseparators and electrodes, a solvent and/or and polymer can induceeither chemical or morphological changes, and/or loss of conductivity ininorganic conductors. For example, sulfidic inorganic conductorsincluding argyrodite-like inorganics can be degraded by polar polymersand/or polar solvents.

Another challenge addressed by the disclosure herein is the instabilityof sulfidic materials in composite electrolytes in moderately polar andvery polar solvents. Table 1, below, shows the effect of solventpolarity on the stability of sulfidic materials.

TABLE 1 Effect of solvent polarity on the stability of sulfidicmaterials Stability of Polarity Index Sulfidic Materials of Solvent (P)Example of Solvent (P) Very Unstable >4.5 NMP (6.7) Acetonitrile (5.8)Acetone (5.1) Methyl Ethyl Ketone (4.7) Unstable* >3.5-4.5 Ethyl Acetate(4.4) THF (4.0) Chloroform (4.1) n-Butyl Alcohol (3.9) Stable   0-3.5Dichloromethane (3.1) Chlorobenzene (2.7) Xylene (2.5) Cyclohexane (0.2)Pentane (0.0) *Sulfidic materials are stable in halogenated solvents inthis range including chloroform

While glass materials (such as LPS glasses) are susceptible to polarsolvents or polymers induced crystallization, which can cause severelosses in conductivities, crystalline argyrodites have better retentionof conductivities. Thus, in some embodiments, argyrodite-containingcomposites can be prepared with various polymeric binders, includingvery polar ones, as long as the process is be done without the use ofpolar solvents that degrade the inorganic. Examples of such bindersinclude poly(vinylacetate), nitrile butadiene rubber having up to 30%nitrile groups, poly(acrylonitrile-co-styrene-co-butadiene) (ABS),poly(ethylene-co-vinylacetate), poly(styrene-co-acrylonitrile) (SAN),poly(styrene-co-maleic anhydride), poly(meth)acrylates, poly(alkyeneglycols), poly(butadiene-co-acrylate), poly(butadiene-co-acrylicacid-co-acrylonitrile), poly(ethylene-co-acrylates), polyethers,polyesters of dialkyl phthalates, or poly(vinyl chloride) (PVC).

Embodiments described herein include polymeric binders that include oneor more types of functional groups. The functional groups can improveone or more of the following: solubility in organic solvents, adhesionto inorganic particles, adhesion to current collectors, dispersibilityof inorganic particles, mechanical performance, ionic conductivity, andelectronic conductivity.

In particular embodiments, a non-polar binder such as SEBS is modifiedwith a small amount of a polar functional group. The resulting binderhas mechanical properties tailored for use in a composite. In particularembodiments, a polar binder such as PVDF is modified with a functionalgroup. The resulting binder is soluble in less polar solvents.

Functionalized Polymeric Binder

A polymer of polymer binder has a backbone that may be functionalized.As described above, In some embodiments, the polymer backbone isnon-polar. Examples include copolymers (block, gradient, random, etc.)such as styrene-butadiene-styrene (SBS), styrene-isoprene-styrene (SIS),styrene-ethylene/propylene-styrene (SEPS),styrene-ethylene-butylene-styrene (SEBS), styrene butadiene rubber(SBR), ethylene propylene diene monomer (EPDM) rubber, and homopolymerssuch as polybutadiene (PBD), polyethylene (PE), polypropylene (PP), andpolystyrene (PS). In some embodiments, the polymer is polar withexamples including acrylonitrile-butadiene-styrene (ABS), nitrile rubber(NBR), ethylene vinyl acetate (EVA) copolymers, oxidized polyethylene.Additional examples include fluorinated polymers such as PVDF,polytetrafluoroethylene, and perfluoropolyether (PFPE) and siliconessuch polydimethylsiloxane (PDMS).

Functional Groups

Functional groups include, but are not limited to aromatic, alkyl(saturated and unsaturated, such as in alkenyl or alkynyl), alcohols(—OH), amines (—N—R₁R₂, in which R₁ and R₂ is, independently, H,optionally substituted alkyl, or optionally substituted aryl, or R₁ andR₂, taken together with the nitrogen atom to which each are attached,form a heterocyclyl group), heterocyclyl (e.g., substituted furanyl,thiophenyl, or pyrrolyl), carboxylic acid (—C(═O)OH), carboxylate salts(—C(═O)O⁻M⁺), carboxylic acid esters (C(═O)O—R), amides (—C(═O)NR₁R₂),ethers (—OR), thiols (—SH), thioethers (—S—R), disulfides (—SS—R), nitro(—NO₂), sulfonic acid (—S(═O)₂OH), sulfonates (—S(═O)₂O⁻M⁺), sulfonicacid esters (—S(═O)₂OR), sulfoxides (—S(═O)₂R), sulfinic acid(—S(═O)OH), sulfinates (—S(═O)O⁻M⁺), sulfinic acid esters (—S(═O)OR),sulfinamide (—S(═O)NR₁R₂), sulfonamides (—S(═O)₂NR₁R₂), nitrile (—CN),azide (—N₃), anhydrides (—C(═O)OC(═O)R), ketones (—C(═O)R), aldehydes(—C(O)H), phosphate acids, salts and esters (—OP(═O)(OR)₂), phosphonateacids, salts and esters (—P(═O)(OR)₂), phosphinate acids, salts andesters (—P(—R)(═O)OR), phosphines (—P(═O)(—R)₃), amides and amido-estersof phosphates, phosphonates, phosphinates and phosphines, carbonates,cyclic esters, cyclic anhydrides, β-keto acids, esters and salts, maleicacid, esters, salts anhydrides, maleimides, malamides, and succinic acidderivatives. Examples are below.

where R, R₁, R₂, R₃ are independently for each occurrence selected from—CN, —H, —OH, a metal cation Me⁺, —OMet optionally substituted aryl,optionally substituted alkoxy, optionally substituted alkyl, optionallysubstituted alkenyl, and optionally substituted alkynyl; and X isindependently for each occurrence selected from —F, —Cl, —Br, and —I;and n is an integer from 1 to 10. Examples of metal cations Me⁺ includeLi⁺, Na⁺ and K⁺. In some instances, the metal cation Me⁺ interacts witha non-carbon heteroatom (e.g., O, N, S, etc.).

The functional groups can be incorporated during polymerization stepand/or in a post-polymerization functionalization step. Polymers can beprepared with one or multiple types of functional groups, depending ontargeted features of the binder. The properties include but are notlimited to: solubility in organic solvents, adhesion to inorganicparticles, adhesion to current collectors, dispersibility of inorganics,mechanical performance, ionic conductivity, electrochemical and chemicalstabilities, and electronic conductivity.

In particular examples, non-polar backbones may be functionalized withpolar groups to improve mechanical performance. Functionalization ofnon-polar backbones such as SEBS with groups such as maleic anhydrideand furfurylamine described further below.

In some embodiments, the polymer binder has a polar backbone. Polarbackbones such as PVDF and NBR may be functionalized with functionalgroups to improve solubility in solvents having a lower P index.Functional groups include, but are not limited, to fully and partiallysaturated and unsaturated linear, branched or cyclic hydrocarbons, i.e.:n-butyl, n-hexyl, n-dodecyl, 2-ethylhexyl, cyclohexyl, palmitoyl,linoleoyl, or butenyl groups. Other, non-polar groups include aromatics,such as phenyl, benzyl, naphthalene functionalities. In addition,functional groups with higher polarity can be used as well, as long asthey are soluble in solvents with specific P index (Table 1). Examplesinclude, but are not limited to, various mono-, di-, oligo- andpolyesters, such as esters of fatty acids or higher C alcohols, i.e.:palmitates, myristates or dodecanol esters, polyesters, i.e:poly(lauryllactone)-block-polytetrahydrofuran, or other polymers, likepoly(methyl methacrylate), poly(2-ethylhexyl acrylate).Functionalization of PVDF with non-polar groups such as styrene isdescribed further below.

In some embodiments, binders are functionalized to improve adhesion tocurrent collectors. In some embodiments, a binder may be functionalizedwith silanes to improve adhesion to metal current collectors,particularly to aluminum and copper. In some embodiments, a binder maybe functionalized with acidic functionalities such as phosphates orcarboxylates that bond to the surface of metals via chemical reaction.In addition, adhesion can be enhanced via physical interactions, such ashydrogen bonding or ion coordination, that can occur between speciespresent on the surface of current collectors and binder functionalitiessuch as alcohols, amides, and esters.

In some embodiments, binders are functionalized to improve themechanical properties of composites and their processability. Thepresence of polar groups might induce ionic conductivity in polymerphase, particularly if mixed with lithium salts, i.e. LiPF₆, LiTFSI,LiClO₄, etc. However, in many embodiments, the ionic conduction throughthe polymer phase is expected to be orders of magnitude lower than thatof inorganic conductor and hence have negligible contribution to totalionic conductivity. This may generally the case unless polymer isspecifically engineered to be ionically conductive.

Hydrophobic Binders Modified With Polar Groups

In some embodiments, the polymer binder is a thermoplastic elastomersuch as SEBS, SBS, or SIS. The low polarity and hydrophobic character ofsuch binders allow for high retention of initial conductivity of pureinorganic conductors, such as LPS glasses or argyrodites.

In some embodiments, the polymer binder backbone is SEBS. SEBS is asaturated version of SBS. Saturation reduces unwanted chemical reactionswith inorganics or, on electrodes, gelation and improves thermalstability. This is especially true for SBS with high 1,2-vinyl content.Pure PBD (0% styrene) is a rubbery material, where pure PS is a brittleresin. A copolymer of these such as SBS or SEBS shows mixed propertieswith the plastic and elastic behavior controlled by the volume ratio ofthe components. According to various embodiments, SBS or SEBS having astyrene volume fraction of 10%-90%, or more particularly 15%-65%, can beused. The triblock polymeric backbone provides high elasticity andmechanical strength, despite highly hydrophobic composition. Polyolefinand polystyrene blocks rely on London and π-π forces and interact veryweakly with inorganic conductor particles. Therefore, relatively lowpressures and temperatures (above Tg of polystyrene) are sufficient tobreak physical bonds between the binder and the surface of theinorganic, enabling interparticle contact and hence high conductivitiesin composite electrolytes. However, weak particle-polymer interactionssignificantly affect contact between phases, decreasing mechanicalproperties of the composite and possibly leading to issues with wetting,adhesion, and delamination.

Provided herein are hydrophobic binders modified with small fractions ofpolar groups (on the level of few %, for example, 0.5-5%) andsuccessfully used as binders in hybrid electrolytes that show improvedmechanical performance while maintaining acceptable room temperatureionic conductivities.

A thermoplastic elastomer such as SEBS, SBS, or SIS may be modified witha polar group such as maleic anhydride or furfurylamine. Examples 1 and2 below describe the increase in modulus, tensile strength, andelongation at break for modified SEBS binders.

Polar Binders Modified With Non-Polar Groups

In some embodiments, the polymer binder backbone is a polar polymer suchas PVDF or NBR. In some embodiments, polar polymers are functionalizedto improve solubility in solvents that are compatible with the inorganicconductor. In some embodiments, the polar polymers are functionalized toimprove compatibility with the inorganic conductor.

In composite materials, including electrolyte separators and electrodes,a solvent and/or and polymer can induce either chemical or morphologicalchanges, and/or loss of conductivity in inorganic conductors. Forexample, sulfidic inorganic conductors as Li₂S—P₂S₅, Li₂S—P₂S₅—LiX,Li₂S-P₂S₅—Li₂O, LiX—P₂S₅—Li₃O₄glasses, glass-ceramics and ceramics, aswell as argyrodite-like inorganics can be degraded by polar solventsand/or polar polymers.

Very and moderately polar solvents such as NMP, DMF, DMSO, ethanol, THF,acetone, ethyl acetate should be avoided to prevent loss of conductivityor other undesirable changes. Lower polarity solvents, includinghydrocarbons (pentanes, hexanes, heptanes, cyclohexane), aromatics(toluene, xylene, trimethylbenzenes), chlorinated aromatics andhydrocarbons (chlorobenzene, dichlorobenzenes, dichloromethane,dichloroethanes, chloroform), higher C esters, ethers and ketones(2-ethylhexyl acetate, butyl butyrate, dibutyl ether, cyclohexanone),may be used as they do not affect inorganic conductors. Table 1, above,provides guidelines for polarity index of solvents that may be used insome embodiments.

Moderately polar binders, like NBR, have no or poor solubility in withP<3.5 solvents and typically require solvents with P of about 4, likeTHF or acetone. In case of very polar binders like PVDF, only solventslike NMP (P=6.7) can dissolve them. In some embodiments, polar bindersfunctionalized functional groups that decrease their polarity andproviding improved solubility in sulfide-compatible solvents areprovides. That is, binders such as NBR or PVDF, are functionalized withnon-polar groups to improve their solubility in solvents with lower Pindex. In some embodiments, up to 50 wt. % of a binder is the functionalgroup.

In some embodiments, a modified PVDF binder is provided. PVDF modifiedeither directly during synthesis, i.e. direct copolymerization withstyrene (Scheme 1A) or with radical-active monomer such aschlorotrifluoroethylene (Scheme 1B). In addition, PVdF can be modifiedin post-functionalization processes, such as ozone pretreatment to formoxides or base treatment to incorporate double bonds.

Scheme 1. Incorporation of polystyrene into PVdF via (A) directcopolymerization with styrene, (B) grafting from PVdF copolymerized withchlorotrifluoroethylene, and (C) radical styrene grafting frombase-treated PVdF.

Table 2, below, shows examples of polymers that have low solubility innon-polar solvents and may be functionalized to improve solubility foruse as polymeric binders in composites.

TABLE 2 Polymers and solubility Polymer Polarity SolubilityPolyoxymethylene (POM) Polar Low solubility in non-polar solventsPolyamides (PA): aliphatic Polar Some, e.g. nylon, low polyamides suchNylon-6, solubility in non-polar Nylon-66, etc.; solvents semi-aromaticpolyamides such as polyphthalamides, PA-6T, etc.; aromatics polyamidessuch as aramids, etc. Polyaryletherketone such Polar Low solubility innon-polar as polyetheretherketone solvents (PEEK), etc. Polyimide (PI)Polar Low solubility in non-polar solvents Polyamide-imide (PAI) PolarLow solubility in non-polar solvents Polyesters such as Polar Soluble insome polar polyethylene terephthalate solvents; low solubility in (PET),Polybutylene some non-polar solvents terephthalate (PBT), Polybutyleneadipate terephthalate (PBAT), etc. Poly(vinyl chloride) (PVC) PolarSoluble in some polar solvents; low solubility in some non-polarsolvents Poly(methyl methacrylate) Polar Soluble in some polar (PMMA)solvents; low solubility in some non-polar solvents Cellulose acetate(CA) Polar Soluble in some polar solvents; low solubility in somenon-polar solvents Polyvinylidene fluoride Polar Soluble in some polar(PVDF) solvents; low solubility in non-polar solvents Polyethylene oxide(PEO) Polar Soluble in some polar solvents; limited solubility in somenon-polar solvents Polypropylene oxide (PPO) Polar Soluble in some polarsolvents; limited solubility in some non-polar solvents Polysulfone(PSU) Polar Soluble in some non-polar solvents; low solubility in somenon-polar solvents Polyurethane (PU) Polar Soluble in some non-polar andpolar solvents Polyethersulfone (PES) Polar Soluble in some polarsolvents; low solubility in some non-polar solvents Polyetherimide (PEI)Polar Soluble in some polar solvents; low solubility in some non-polarsolvents Acrylonitrile Butadiene Polar Soluble in some polar Styrene(ABS) solvents; low solubility in some non-polar solvents Polycarbonate(PC) Polar Soluble in some polar solvents; low solubility in somenon-polar solvents Poly(vinyl acetate-co- Polar Soluble in some polarethylene) (PVAE) solvents; low solubility in some non-polar solventsPoly(vinyl alcohol) (PVA) Polar Soluble in some non-polar solvents; lowsolubility in some non-polar solvents Nitrile butadiene rubber PolarDepends on the amount of (NBR) nitrile groups—soluble in some non-polarsolvents; low solubility in some non-polar solvents. Polyacrylonitrile(PAN) Polar Soluble in some polar solvents; low solubility in somenon-polar solvents

EXAMPLES Example 1 Elastic Modulus of SEBS, SEBS-gMA, and SEBS-gFA

SEBS modified with 2% maleic anhydride (SEBS-gMA) and SEBS-gMAfunctionalized with furfurylamine (SEBS-gFA). SEBS-gFA was synthesizedby reacting SEBS-gMA with and excess of furfuryl amine as shown inscheme 1.

In a glove box operated under nitrogen, 30.0 g (6.1 mmol of maleicanhydride) ofpolystyrene-b-poly(ethylene-ran-butylene)-b-polystyrene-g-maleicanhydride (SEBS-gMA, Sigma-Aldrich) and 250 g of dry toluene were placedin a 500 ml pressure vessel dried at 145° C. prior to use. The flask wassealed, and the mixture was stirred on a hot-plate at 60° C. until thepolymer fully dissolved. Next, the flask was brought back into the boxand cooled to room temperature before 2.4 g (24.7 mmol) of furfurylaminewas slowly added in to the mixture. The reaction was further stirred at60° C. for 18 hrs. Afterward the reaction mixture was precipitated intomethanol, solids were re-dissolved in dichloromethane and precipitatedagain into methanol; the process was repeated two more times to obtainthe furfuryl-modified SEBS (SEBS-gFA) as white solid. The product wasdried under vacuum at 100° C. for 16 hrs. The wt. % of the functionalgroups in the SEBS-gFA was 3.5%.

Tensile testing of the crosslinked film was performed to determine theelastic modulus, tensile strength and elongation at break. Theproperties of SEBS-gMA and SEBS-gFA films were measure against SEBS filmprocessed under the same conditions. All films were cut into 8 mm×50 mmstrips and at least three measurements per film were performed using amini tensile tester. Due to the short grip separation of the instrument,the tensile strength and elongation at break could not be measured asthe limit of the instrument was reached before the failure of thematerials occurred. Each of the polymer films was very elastic,reaching >800% elongation. Table 3 summarizes elastic moduli extractedfrom stress-strain curves for SEBS, SEBS-gMA, and SEBS-gFA films.

TABLE 3 Elastic moduli of different polymer films. SEBS SEBS-gMASEBS-gFA E/MPa 12.07 ± 0.14 20.82 ± 2.96 26.82 ± 1.65Elastic moduli measured for SEBS, SEBS-gMA, and SEBS-gFA varysignificantly from each other, providing evidence of the importance ofthe overall composition and type of functional group. Adding 2 wt. % ofpolar maleic anhydride grafts to SEBS composition drastically increasedthe modulus of the binder, showing over 70% higher value than unmodifiedSEBS. Further modification of SEBS-gMA with furfuryl groups resulted inSEBS-gFA binder with even higher modulus of 26.82 MPa.

Example 2 Composite Electrolytes Including SEBS, SEBS-gMA, and SEBS-gFAas Binders

After testing mechanical properties of pure SEBS, SEBS-gMA, and SEBS-gFAthe polymers were incorporated into composite electrolytes. Each polymerwas tested as a binder in hybrids prepared with 80 wt. % of75:25=Li₂S:P₂S₅ sulfide glass. SEBS and SEBS-gMA were also incorporatedinto composite electrolytes prepared with 80 wt. % Li_(5.6)PS_(4.6)Cl1.4argyrodite. Composites were prepared as thin films via slurry casting,dried and hot-pressed at 160° C. Binder structures are provided below:(A) SEBS; (B) SEBS-gMA, and (C) SEBS-gFA.

Conductivities of the composites were measured to assess the effect ofbinder on the conductivity retention of pure 75:25=Li₂S:P₂S₅ sulfideglass. The incorporation of polar groups into non-polar binder, such asSEBS, had a drastic effect on conductivity of measured films. When SEBSwas used as a binder, the conductivity was about 0.18 mS/cm, showinghigh (33%) conductivity retention of the original inorganic materials(about 0.55 mS/cm) (Table 3).

SEBS was modified with small amounts of polar functionalities capable ofstrong binding to the surface of glass particles resulted conductivitiesdropped by nearly an order of magnitude (Table 5). The composite withSEBS and SEBS-gMA mixed binders (1:4, w/w) showed good conductivity of0.102 mS/cm (Table 5), providing evidence that the ionic conductivity ofcomposite electrolytes drops exponentially with increasing fraction ofSEBS-gMA in 20 wt. % total of polymer phase. The trend shows a lineardrop in conductivity on a semi-logarithmic scale. When pure SEBS-gFA wasused as the organic matrix, the conductivity was only lower by thefactor of 2.3×. In case of argyrodite composites, conductivity forSEBS-gMA was about 30% lower as compared to about 90% observed in glasscomposites. These results show that glassy materials are susceptible topolar solvents or polymers induced crystallization, which causes severelosses in conductivities. On the other hand, crystalline argyroditesshow better retention of conductivities (as compared to composites withnon-polar SEBS binder, not the actual inorganic powder) as they do notsuffer from conductivity loss during crystallization process.

In some embodiments, argyrodite (or other crystalline sulfidicconductors) composites can be prepared with various polymeric binders,including very polar ones, as long as the process is be done without theuse of polar solvents that degrade the inorganic. Table 4 belowsummarizes composites prepared with 5 wt. % binders (95 wt. %argyrodite) with increasing polarity, SEBS-gMA, NBR₂₀ (20% nitrilegroups) and poly(vinyl acetate) (PVAc), that show conductivities betweenabout 0.5 mS/cm and 0.7 mS/cm. There is a drop in conductivities ofcomposites with more polar binders, but it is not as drastic as in caseof glasses. Produced composites maintain good conductivies, while havingbetter mechanical properties.

TABLE 4 Conductivity of argyrodite-containing composites Conductivity atConductor composition Polymer binder 25° C./mS · cm⁻¹Li_(5.6)PS_(1.4)Cl_(1.4) SEBS-gMA 0.705 NBR₂₀ 0.606 PVAc 0.508

Mechanical testing of all composites was done to obtain elastic modulus,tensile strength and elongation at break. Mechanical testing wasperformed under the same conditions as for the pure polymer films.Modulus, tensile strength and elongation at break values were extractedfrom stress-strain curves and summarized in Table 5.

TABLE 5 Conductivity and mechanical properties measured for hybrids with80 wt. % 75:25 = Li₂S:P₂S₅ glass or Li_(5.6)PS_(4.6)Cl_(1.4) argyroditesand different polymer binders (20 wt. %) Tensile Elongation ConductorPolymer Strength/ at break/ Cond. at comp. binder Modulus/GPa MPa % 25°C./mS · cm⁻¹ Li₂S:P₂S₅ = SEBS 0.575 ± 0.116 4.24 ± 0.68  2.20 ± 0.330.182 75:25 SEBS-gMA 0.646 ± 0.107 5.56 ± 0.08  4.47 ± 0.27 0.023 (80wt. %) SEBS:SEBS- — — — 0.102 gMA (4:1) SEBS-gFA 0.606 ± 0.065 8.29 ±0.27 17.00 ± 0.30 0.078 Li_(5.6)PS_(1.4)Cl_(1.4) SEBS 0.815 ± 0.060 5.74± 0.13  1.98 ± 0.19 0.325 (80 wt. %) SEBS-gMA 0.758 ± 0.105 11.6 ± 0.0020.24 ± 2.24 0.213

Visual comparison of stress-strain curves obtained for composites withdifferent binders showed a clear difference in mechanical properties.Increasing tensile strength and elongation at break of compositesprepared with higher polarity binders. In the case of SEBS onlycomposites, the samples break at only about 2% elongation. WhenSEBS-gMA, containing as little as 2 wt. % of maleic grafts, isincorporated into a composite the value doubles reaching 4.5% for75:25=Li₂S:P₂S₅glass composite. The elasticity of the compositeincreases even more, up to about 10 times, for argyrodite-containingcomposites, providing 20.24% elongation. Further modification withfurfuryl groups (SEBS-gFA) increased the wt. % of polar groups to 3.5wt. %. That modification drastically increased the elongation at breakto 17.0% for 75:25=Li₂S:P₂S₅ glass composite, which is respectively 8.5and 4 times higher than in case of SEBS and SEBS-gMA. The same trend wasobserved for tensile strength of films, which showed 4.2, 5.6 and 8.3MPa values for SEBS, SEBS-gMA and SEBS-gFA binder respectively,providing evidence of improved resistance of films to breakage when morepolar binder is incorporated into organic matrix.

Similar observations were made for argyrodite films where ultimatestrength changed from 5.74 to 11.6 MPa when binder was changed from SEBSto SEBS-gMA. The elastic modulus of was barely dependent on the type ofbinder, varying between 0.57-0.65 GPa for glasses and 0.76-0.82 GPa forargyrodite composites.

The composites in Table 5 have lower conductivity than those in Table 4due to the higher polymer loading. However, the conductivity retentionof the argyrodite-containing composites is clear. In some embodiments,argyrodites in a polar polymer may have conductivities of at least 0.2mS·cm⁻¹ at 25° C., at least 0.25 mS·cm⁻¹ at 25° C., or least 0.35mS·cm⁻¹ at 25° C. with a maximum ionically conductive particle contentof 90wt %, 85wt %, or 80 wt %. At the same time, mechanical propertiesmay be good due to the presence of polar groups, e.g., elongation atbreak is at least 5%, 10%, 15%, or 20%.

The data shows that properties of composite electrolytes can be finelytuned by controlling the composition of both organic and inorganicphases. The subtle changes to chemical composition of binder can havetremendous effect on properties of resulting composites. The mechanicalstrength and elasticity can be increased several times by adding aslittle as 2% of polar functional groups, while conductivity can remainin acceptable room temperature range.

Inorganic Phase

The inorganic phase of the composite materials described herein conductsalkali ions. In some embodiments, it is responsible for all of the ionconductivity of the composite material, providing ionically conductivepathways through the composite material.

The inorganic phase is a particulate solid-state material that conductsalkali ions. In the examples given below, lithium ion conductingmaterials are chiefly described, though sodium ion conducting or otheralkali ion conducting materials may be employed. According to variousembodiments, the materials may be glass particles, ceramic particles, orglass ceramic particles. The methods are particularly useful forcomposites having glass or glass ceramic particles. In particular, asdescribed above, the methods may be used to provide composites havingglass or glass ceramic particles and a polar polymer without inducingcrystallization (or further crystallization) of the particles.

The solid-state compositions described herein are not limited to aparticular type of compound but may employ any solid-state inorganicionically conductive particulate material, examples of which are givenbelow.

In some embodiments, the inorganic material is a single ion conductor,which has a transference number close to unity. The transference numberof an ion in an electrolyte is the fraction of total current carried inthe electrolyte for the ion. Single-ion conductors have a transferencenumber close to unity. According to various embodiments, thetransference number of the inorganic phase of the solid electrolyte isat least 0.9 (for example, 0.99).

The inorganic phase may be an oxide-based composition, a sulfide-basedcomposition, or a phosphate-based composition, and may be crystalline,partially crystalline, or amorphous. As described above, the certainembodiments of methods are particularly useful for sulfide-basedcompositions, which can degrade in the presence of polar polymers.

In certain embodiments, the inorganic phase may be doped to increaseconductivity. Examples of solid lithium ion conducting materials includeperovskites (e.g., Li_(3x)La_((2/3)-x)TiO₃, 0≤x≤0.67), lithium superionic conductor (LISICON) compounds (e.g., Li_(2+2x)Zn_(1−x)GeO₄, 0≤x≤1;Li₁₄ZnGe₄O₁₆), thio-LISICON compounds (e.g., Li_(4−x)A_(1−y)B_(y)S₄, Ais Si, Ge or Sn, B is P, Al, Zn, Ga; Li₁₀SnP₂S₁₂), garnets (e.g.Li₇La₃Zr₂O₁₂, Li5La₃M₂O₁₂, M is Ta or Nb); NASICON-type Li ionconductors (e.g., Li_(1.3)Al_(0.3)Ti_(1.2)(PO₄)₃), oxide glasses orglass ceramics (e.g., Li₃BO₃—Li₂SO₄, Li₂O—P₂O₅, Li₂O—SiO₂), argyrodites(e.g. Li₆PS₅X where X═Cl, Br, I), sulfide glasses or glass ceramics(e.g., 75Li₂S-25P₂S₅, Li₂S—SiS₂, LiI—Li₂S—B₂S₃) and phosphates (e.g.,Li_(1−x)Al_(x)Ge_(2−x)(PO₄)₃ (LAGP), Li_(1+s)Ti_(2−x)Al_(x)(PO₄)).Further examples include lithium rich anti-perovskite (LiRAP) particles.As described in Zhao and Daement, Jour J. Am. Chem. Soc., 2012, 134(36), pp 15042-15047, incorporated by reference herein, these LiRAPparticles have an ionic conductivity of greater than 10⁻³S/cm at roomtemperature.

Examples of solid lithium ion conducting materials include sodium superionic conductor (NASICON) compounds (e.g., Na_(1+x)Zr₂Si_(x)P_(3−x)O₁₂,0<x<3). Further examples of solid lithium ion conducting materials maybe found in Cao et al., Front. Energy Res. (2014) 2:25 and Knauth, SolidState Ionics 180 (2009) 911-916, both of which are incorporated byreference herein.

Further examples of ion conducting glasses are disclosed in Ribes etal., J. Non-Cryst. Solids, Vol. 38-39 (1980) 271-276 and Minami, J.Non-Cryst. Solids, Vol. 95-96 (1987) 107-118, which are incorporated byreference herein.

According to various embodiments, an inorganic phase may include one ormore types of inorganic ionically conductive particles. The particlesize of the inorganic phase may vary according to the particularapplication, with an average diameter of the particles of thecomposition being between 0.1 μm and 500 μm for most applications. Insome embodiments, the average diameter is between 0.1 μm and 100 μm. Insome embodiments, a multi-modal size distribution may be used tooptimize particle packing. For example, a bi-modal distribution may beused. In some embodiments, particles having a size of 1 μm or less areused such that the average nearest particle distance in the composite isno more than 1 μm. This can help prevent dendrite growth. In someembodiments, average particle size is less 10 μm or less than 7 μm. Insome embodiments, a multi-modal size distribution having a first sizedistribution with an average size of less than 7 μm and a second size ofgreater than 10 μm may be used. Larger particles lead to membranes withmore robust mechanical properties and better conductivities, whilesmaller particles give more compact, uniform films with lower porosityand better density.

The inorganic phase may be manufactured by any appropriate method. Forexample, crystalline materials may be obtained using different syntheticmethods such as solution, sol-gel, and solid state reactions. Glasselectrolytes may be obtained by quench-melt, solution synthesis ormechanical milling as described in Tatsumisago, M.; Takano, R.; TadanagaK.; Hayashi, A. J. Power Sources 2014, 270, 603-607, incorporated byreference herein.

As used herein, the term amorphous glass material refers to materialsthat are at least half amorphous though they may have small regions ofcrystallinity. For example, an amorphous glass particle may be fullyamorphous (100% amorphous), at least 95% (vol). amorphous, at least 80%(vol.) amorphous, or at least 75% (vol.) amorphous. While theseamorphous particles may have one or more small regions of crystallinity,ion conduction through the particles is through conductive paths thatare mostly or wholly isotropic.

lonically conductive glass-ceramic particles have amorphous regions butare at least half crystalline, for example, having at least 75% (vol.)crystallinity. Glass-ceramic particles may be used in the compositesdescribed, herein, with glass-ceramic particles having a relatively highamount of amorphous character (e.g., at least 40 (vol) % amorphous)useful in certain embodiments for their isotropic conductive paths. Insome embodiments, ionically conductive ceramic particles may be used.Ionically conductive ceramic particles refer to materials that aremostly crystalline though they may have small amorphous regions. Forexample, a ceramic particle may be fully crystalline (100% vol.crystalline) or at least 95% (vol). crystalline.

In some embodiments, the inorganic phase includes argyrodites. Theargyrodites may have the general formula:

A_(7−x)PS_(6−x)Hal_(x)

A is an alkali metal and Hal is selected from chlorine (CI), bromine(Br), and iodine (I).

In some embodiments, the argyrodite may have a general formula as givenabove, and further be doped. An example is argyrodites doped withthiophilic metals:

A_(7−x−(z*m))M^(z) _(m)PS_(6−x)Hal_(x)

wherein A is an alkali metal; M is a metal selected from manganese (Mn),iron (Fe), cobalt (Co), nickel (Ni), copper (Cu), zinc (Zn), and mercury(Hg); Hal is selected from chlorine (Cl), bromine (Br), and iodine (I);z is the oxidation state of the metal; 0≤x≤2; and 0≤m<(7-x)/z. In someembodiments, A is lithium (Li), sodium (Na) or potassium (K). In someembodiments, A is Li. Metal-doped argyrodites are described further inU.S. patent application Ser. No. 16/829,962, incorporated by referenceherein. In some embodiments, the composite may include oxideargyrodites, for example, as described in U.S. patent application Ser.No. 16/576,570, incorporated by reference herein. Alkali metalargyrodites include argyrodites of the formulae given above as well asargyrodites described in US Patent Publication No. 20170352916 whichinclude Li_(7−x+y)PS_(6−x)Cl_(x+y) where x and y satisfy the formula0.05≤y≤0.9 and −3.0x+1.8≤y≤−3.0x+5, or other argyrodites withA_(7−x+y)PS_(6−x)Hal_(x+y) formula. Such argyrodites may also be dopedwith metal as described above, which include A_(7−x+y−(z*m))M^(z)_(m)PS_(6−x)Hal_(x+y).

The mineral Argyrodite, Ag₈GeS₆, can be thought of as a co-crystal ofAg₄GeS₄ and two equivalents of Ag₂S. Substitutions in both cations andanions can be made in this crystal while still retaining the sameoverall spatial arrangement of the various ions. In Li₇PS₆, PS₄ ³⁻ ionsreside on the crystallographic location occupied by GeS₄ ⁴⁻ in theoriginal mineral, while S²⁻ ions retain their original positions and Li⁺ions take the positions of the original Ag⁺ ions. As there are fewercations in Li₇PS₆ compared to the original Ag₈GeS₆, some cation sitesare vacant. These structural analogs of the original Argyrodite mineralare referred to as argyrodites as well.

Both Ag₈GeS₆ and Li₇PS₆ are orthorhombic crystals at room temperature,while at elevated temperatures phase transitions to cubic space groupsoccur. Making the further substitution of one equivalent of LiCI for oneLi₂S yields the material Li₆PS₅Cl, which still retains the argyroditestructure but undergoes the orthorhombic to cubic phase transition belowroom temperature and has a significantly higher lithium-ionconductivity. Because the overall arrangement of cations and anionsremains the same in this material as well, it is also commonly referredto as an argyrodite. Further substitutions which also retain thisoverall structure may therefore also be referred to as argyrodites.Alkali metal argyrodites more generally are any of the class ofconductive crystals with alkali metals occupying Ag⁺ sites in theoriginal Argyrodite structure, and which retain the spatial arrangementof the anions found in the original mineral.

In one example, a lithium-containing example of this mineral type,Li₇PS₆, P5₄ ³⁻ ions reside on the crystallographic location occupied byGeS₄ ⁴⁻ in the original mineral, while S² ions retain their originalpositions and Li⁺ ions take the positions of the original Ag⁺ ions. Asthere are fewer cations in Li₇PS₆ compared to the original Ag₈GeS₆, somecation sites are vacant. As indicated above, making the furthersubstitution of one equivalent of LiCl for one Li₂S yields the materialLi₆PS₅Cl, which still retains the argyrodite structure. FIG. 2 shows acubic argyrodite Li₆PS₅Cl. In the example of FIG. 2, Li⁺ occupies the 4⁺sites in the Argyrodite mineral, PS₄ ³⁻ occupies the GeS₄ ⁴⁻ sites inthe original, and a one to one ratio of S²⁻ and Cl⁻ occupy the twooriginal S²⁻ sites.

There are various manners in which substitutions may be made that retainthe overall argyrodite structure. For example, the original mineral hastwo equivalents of S²⁻, which can be substituted with chalcogen ionssuch as 0²⁻, Se²⁻, and Te²⁻. A significant fraction of the of S²⁻ can besubstituted with halogens. For example, up to about 1.6 of the twoequivalents of S²⁻ can be substituted with Cl⁻, Br, and 1⁻¹, with theexact amount depending on other ions in the system. While Cl⁻is similarin size to S²⁻, it has one charge instead of two and has substantiallydifferent bonding and reactivity properties. Other substitutions may bemade, for example, in some cases, some of the 5²⁻ can be substitutedwith a halogen (e.g., Cl⁻) and the rest replaced with Se²⁻. Similarly,various substitutions may be made for the GeS₄ ³⁻ sites. PS₄ ³⁻ mayreplace GeS₄ ³⁻; also PO₄ ³⁻, PSe₄ ³⁻, SiS₄ ³⁻, etc. These are alltetrahedral ions with four chalcogen atoms, overall larger than S²⁻, andtriply or quadruply charged.

In other examples, which will be compared to the Li₆PS₅Cl argyroditestructure described above, Li₆PS₅Br and Li₆PS₅I substitute largerhalides in place of the chloride, e.g., Li₆PO₅Cl and Li₆PO₅Br. Z. anorg.Allg. Chem., 2010, no. 636, 1920-1924, incorporated by reference hereinfor the purpose of describing certain argyrodites, contain the halidesubstitutions described as well as exchanging every sulfur atom in thestructure, in both the S²⁻ and P5₄ ³⁻ ions, for oxygen. The phosphorusatoms in the P5₄ ³⁻ ions found in most examples of lithium-containingargyrodites can also be partially or wholly substituted, for instancethe series Li_(7+x)M_(x)P_(1−x)S₆ (M=Si, Ge) forms argyrodite structuresover a wide range of x. See J. Mater. Chem. A, 2019, no. 7, 2717-2722,incorporated by reference herein for the purpose of describing certainargyrodites. Substitution for P can also be made while incorporatinghalogens. For example, Li_(6+x)Si_(x)P_(1−x)S₅Br is stable from x=0 toabout 0.5. See J. Mater. Chem. A, 2017, no. 6, 645-651, incorporated byreference herein for the purpose of describing certain argyrodites.Compounds in the series Li_(7+x)M_(x)Sb_(1−x)S₆(M=Si, Ge, Sn), where amixture of SbS₄ ³⁻ and MS₄ ⁴⁻ are substituted in place of PS₄ ³⁻ and I⁻is used in place of Cl⁻, have been prepared and found to form theargyrodite structure. See J. Am. Chem. Soc., 2019, no. 141, 19002-19013,incorporated by reference herein for the purpose of describing certainargyrodites. Other cations besides lithium (or silver) can also besubstituted into the cation sites. Cu₆PS₅Cl, Cu₆PS₅Br, Cu₆PS₅I,Cu₆AsS₅Br, Cu₆AsS₅I, Cu_(7.82)SiS_(5.82)Br_(0.18), Cu₂SiS₅I,Cu_(7.49)SiS_(5.49)I_(0.51), Cu_(2.44)SiSe_(5.44)I_(0.56),Cu_(7.75)GeS5.75Br_(0.25), Cu_(7.52)GeS_(5.52)I_(0.48) andCu_(2.52)GeSe_(5.52)I_(0.48) have all been synthesized and haveargyrodite crystal structures. See Z. Kristallogr, 2005, no. 220,281-294, incorporated by reference herein for the purpose of describingcertain argyrodites. From the list of examples, it can be seen that notonly can single elements be substituted in any of the various parts ofthe argyrodite structure, but combinations of substitutions also oftenyield argyrodite structures. These include argyrodites described in USPatent Publication No. 20170352916 which includeLi_(7−x+y)PS_(6−x)Cl_(x+y) where x and y satisfy the formula 0.05≤y≤0.9and −3.0x+1.8≤y≤−3.0x+5.7.

The argyrodites used in the compositions herein described includesulfide-based ion conductors with a substantial (at least 20%, and oftenat least 50%) of the anions being sulfur-containing (e.g., S²⁻ and PS₄³⁻). Sulfide-based lithium argyrodite materials exhibit high Li⁺mobility and are of interest in lithium batteries. As indicated above,an example material in this family is Li₆PS₅Cl, which is a ternaryco-crystal of Li₃PS₄, Li₂S, and LiCl. Various embodiments of argyroditesdescribed herein have thiophilic metals that may occupy lithium cationsites in the argyrodite crystal structure. In an argyrodite as shown inFIG. 2, each cation is coordinated to two sulfurs which are members ofPS₄ ³⁻ anions, one S²⁻ sulfur anion, and two chloride anions. In someembodiments, a thiophilic metal occupies some fraction of these lithiumcation sites to suppress hydrogen sulfide generation. Thiophilic metalsmay be used to similarly dope other alkali metal a rgyrodites.

Composites

Provided herein are composites including organic phase and non-ionicallyconductive particles. In some embodiments, the organic phase hassubstantially no ionic conductivity, and is referred to as“non-ionically conductive.” Non-ionically conductive polymers describedherein have ionic conductivities of less than 0.0001 S/cm. In someembodiments, the organic phase may include a polymer that is ionicallyconductive in the present of a salt such as Lil. lonically conductivepolymers such as polyethylene oxide (PEO), polypropylene oxide (PPO),polyacrylonitrile (PAN), poly(methyl methacrylate) (PMMA) , which areionically conductive in presence of a salt dissolve or dissociate saltssuch as Lil. Non-ionically conductive polymers do not dissolve ordissociate salts and are not ionically conductive even in the presenceof a salt. This is because without dissolving a salt, there are nomobile ions to conduct.

The polymer loading in the solid phase composites may be relatively highin some embodiments, e.g., being at least 2.5%-30% by weight. Accordingto various embodiments, it may between 0.5 wt %-60 wt % polymer, 1 wt%-40 wt % polymer, or 5 wt %-30 wt %. The solid phase composites form acontinuous film.

In some embodiments, the inorganic conductor is at least 75 wt %, atleast 80 wt %, at least 85 wt %, at least 90 wt %, or at least 95 wt %of the composite. Conductivity increases with increasing content, butmechanical strength can decrease. In some embodiments, the inorganicconductor is between 75wt % and 98wt %, e.g., between 80wt % and 95wt %.The balance of the composite may be polymer.

As indicated above, the composite contains a functionalized polymerbackbone binder. The binder may be a mixture of functionalized andnon-functionalized polymer binders. For example, in some embodiments, abinder may be a mixture of a non-polar polymer (e.g., SEBS) and afunctionalized version of the polymer (e.g., SEBS-gFA). A mixture may be1:9-9:1 wt. % polymer:functionalized polymer according to variousembodiments, e.g., 1:5-5:1, or between 1:4-4:1. An unmodified version ofthe polymer (SEBS) includes unfunctionalized polymers and polymers thatinclude insignificant group of functional groups that do not change theproperties of the polymer. Similarly, in some embodiments, the bindermay be a mixture of two or more polymers having different degrees offunctionalization (e.g., 1wt % and 4wt %).

According to various embodiments, the polymer binder may be essentiallyall of the organic phase of the composite, or at least 95 wt. %, 90 wt.%, at least 80 wt. %, at least 70 wt. %, at least 60 wt. %, or at least50 wt. %, of the composite.

In some embodiments, the composites consist essentially ofion-conductive inorganic particles and the organic phase. However, inalternative embodiments, one or more additional components may be addedto the solid composites.

According to various embodiments, the solid compositions may or may notinclude an added salt. Lithium salts (e.g., LiPF6, LiTFSI), potassiumsalts, sodium salts, etc. can be added to improve ionic conductivity inembodiments that include an ionically conductive polymer such as PEO. Insome embodiments, the solid-state compositions include substantially noadded salts. “Substantially no added salts” means no more than a traceamount of a salt. In some embodiments, the ionic conductivity of thecomposite is substantially provided by the inorganic particles. Even ifan ionically conductive polymer is used, it may not contribute more than0.01 mS/cm, 0.05 mS/cm. or 0.1 mS/cm to the ionic conductivity of thecomposite. In other embodiments, it may contribute more.

In some embodiments, the solid-state composition may include one or moreconductivity enhancers. In some embodiments, the electrolyte may includeone or more filler materials, including ceramic fillers such as Al₂O₃.If used, a filler may or may not be an ion conductor depending on theparticular embodiment. In some embodiments, the composite may includeone or more dispersants. Further, in some embodiments, an organic phaseof a solid-state composition may include one or more additional organiccomponents to facilitate manufacture of an electrolyte having mechanicalproperties desired for a particular application.

In some embodiments, discussed further below, the composites areincorporated into, or are ready to be incorporated into, an electrodeand include electrochemically active material, and optionally, anelectronically conductive additive. Examples of constituents andcompositions of electrodes are provided below.

In some embodiments, the electrolyte may include an electrodestabilizing agent that can be used to form a passivation layer on thesurface of an electrode. Examples of electrode stabilizing agents aredescribed in U.S. Patent 9,093,722. In some embodiments, the electrolytemay include conductivity enhancers, fillers, or organic components asdescribed above.

The composite may be provided as a free-standing film, a free-standingfilm that is provided on a release film, a film that has been laminatedon component of a battery or other device such as an electrode or aseparator, or a film that has been cast onto an electrode, separator, orother component.

A composite film may be of any suitable thickness depending upon theparticular battery or other device design. For many applications, thethickness may be between 1 micron and 250 microns, for example 15microns. In some embodiments, the electrolyte may be significantlythicker, e.g., on the order of millimeters.

In some embodiments, the composites are provided as a slurry or paste.In such cases, the composition includes a solvent to be laterevaporated. In addition, the composition may include one or morecomponents for storage stability. Such compounds can include an acrylicresin. Once ready for processing the slurry or paste may be cast orspread on a substrate as appropriate and dried. According to variousembodiments, the slurries may have about 40wt %-50wt % solids content,e.g., 42wt %-45wt %. The solids content is inorganic particles (e.g.,between 80wt % and 95wt % inorganic conductor and 5wt % and 20wt %polymer.)

In some embodiments, the composites are provided as solid mixtures thatcan be extruded.

Devices

The composites described herein may be incorporated into any device thatuses an ionic conductor, including but not limited to batteries and fuelcells. In a battery, for example, the composite may be used as anelectrolyte separator.

The electrode compositions further include an electrode active material,and optionally, a conductive additive. Example cathode and anodecompositions are given below.

For cathode compositions, the table below gives examples ofcompositions.

Electronic conductivity Constituent Active material Inorganic conductoradditive Organic phase Examples NMC Argyrodites Carbon-based PVDF-PScopolymer NCA (e.g., Li₆PS₅Cl, Activated PVDF:PVDF-PS copolymer LiFePO4Li_(5.6)PS_(4.6)Cl_(1.4), carbons SEBS:PVDF-PS copolymer LiCoO2Li_(5.4)M_(0.1)PS_(4.6)Cl_(1.4), CNTs SEBS Li_(5.8)M_(0.1)PS₅Cl,Graphene SBR Na_(5.8)M_(0.1)PS₅Cl Graphite SIS Carbon fibers NBR Sulfideglasses or Carbon black glass ceramics (e.g., Super C) (e.g., 75Li₂S ·25P₂S₅) Wt % range 65%-88% 10%-33% 1%-5% 1%-5%

According to various embodiments, the cathode active material is atransition metal oxide, with lithium nickel cobalt manganese oxide(LiMnCoMnO₂, or NMC) an example. Various forms of NMC may be used,including LiNi_(0.6)Mn_(0.2)Co_(0.2)O₂ (NMC-622),LiNi_(0.4)Mn_(0.3)Co_(0.3)O₂ (NMC-4330), etc. The lower end of the wt %range is set by energy density; compositions having less than 65 wt %active material have low energy density and may not be useful.

Any appropriate inorganic conductor may be used as described above inthe description of inorganic conductors. Li_(5.6)PS_(4.6)Cl_(1.4) is anexample of an argyrodite with high conductivity.Li_(5.4)Cu_(0.1)PS_(4.6)Cl_(1.4) is an example of an argyrodite thatretains high ionic conductivity and suppresses hydrogen sulfide.Compositions having less than 10 wt % argyrodite have low Li⁺conductivity. Sulfide glasses and glass ceramics may also be used.

An electronic conductivity additive is useful for active materials that,like NMC, have low electronic conductivity. Carbon black is an exampleof one such additive, but other carbon-based additives including othercarbon blacks, activated carbons, carbon fibers, graphites, graphenes,and carbon nanotubes (CNTs) may be used. Below 1 wt % may not be enoughto improve electronic conductivity while greater than 5% leads todecrease in energy density and disturbing active material-argyroditecontacts.

Any appropriate organic phase may be used as described above. Below 1 wt% may not be enough to achieve desired mechanical properties whilegreater than 5% can lead to decrease in energy density and disturbingactive material-inorganic conductor-carbon contacts. In someembodiments, PVDF is used with or without a non-polar polymer.

For anode compositions, the table below gives examples of compositions.

Electronic Primary active Secondary conductivity Constituent materialactive material Inorganic conductor additive Organic phase Examples Si-Graphite Agyrodites (e.g., Carbon-based PVDF-PS copolymer containingLi₆PS₅Cl, Activated PVDF:PVDF-PS active Li_(5.6)PS_(4.6)Cl_(1.4),carbons copolymer materials Li_(5.4)M_(0.1)PS_(4.6)Cl_(1.4), CNTsSEBS:PVDF-PS Elemental Si Li_(5.8)M_(0.1)PS₅Cl, Graphene copolymerSi-carbon Na_(5.8)M_(0.1)PS₅Cl Carbon fibers SEBS composite Sulfideglasses or Carbon black SBR materials glass ceramics (e.g., Super C) SISSialloys, (e.g., NBR e.g., Si 75Li₂S · 25P₂S₅) alloyed with one or moreof Al, Zn, Fe, Mn, Cr, Co, Ni, Cu, Ti, Mg, Sn, Ge Wt % range Si is15%-50% 5%-40% 10%-50% 0%-5% 1%-5%

Hybrid anodes where both Si and graphite are utilized as activematerials deliver higher ICE with increasing graphite content meaningthat ICE of the anode can match ICE of the cathode by adjustingSi/graphite ratio thus preventing irreversible capacity loss on thefirst cycle. ICE can vary with processing, allowing for a relativelywide range of graphite content depending on the particular anode and itsprocessing. In addition, graphite improves electronic conductivity andmay help densification of the anode.

Any appropriate inorganic conductor may be used as described above withrespect to cathodes.

A high-surface-area electronic conductivity additive (e.g., carbonblack) may be used some embodiments. Si has low electronic conductivityand such additives can be helpful in addition to graphite (which is agreat electronic conductor but has low surface area). However,electronic conductivity of Si alloys can be reasonably high making usageof the additives unnecessary in some embodiments. Otherhigh-surface-area carbons (carbon blacks, activated carbons, graphenes,carbon nanotubes) can also be used instead of Super C.

Any appropriate organic phase may be used. In some embodiments, PVDF isused.

Provided herein are alkali metal batteries and alkali metal ionbatteries that include an anode, a cathode, and a compliant solidelectrolyte composition as described above operatively associated withthe anode and cathode. The batteries may include a separator forphysically separating the anode and cathode; this may be the solidelectrolyte composition.

Examples of suitable anodes include but are not limited to anodes formedof lithium metal, lithium alloys, sodium metal, sodium alloys,carbonaceous materials such as graphite, and combinations thereof.Examples of suitable cathodes include, but are not limited to cathodesformed of transition metal oxides, doped transition metal oxides, metalphosphates, metal sulfides, lithium iron phosphate, sulfur andcombinations thereof. In some embodiments, the cathode may be a sulfurcathode.

In an alkali metal-air battery such as a lithium-air battery, sodium-airbattery, or potassium-air battery, the cathode may be permeable tooxygen (e.g., mesoporous carbon, porous aluminum, etc.), and the cathodemay optionally contain a metal catalyst (e.g., manganese, cobalt,ruthenium, platinum, or silver catalysts, or combinations thereof)incorporated therein to enhance the reduction reactions occurring withlithium ion and oxygen at the cathode.

In some embodiments, lithium-sulfur cells are provided, includinglithium metal anodes and sulfur-containing cathodes. In someembodiments, the solid-state composite electrolytes described hereinuniquely enable both a lithium metal anode, by preventing dendriteformation, and sulfur cathodes, by not dissolving polysulfideintermediates that are formed at the cathode during discharge.

A separator formed from any suitable material permeable to ionic flowcan also be included to keep the anode and cathode from directlyelectrically contacting one another. However, as the electrolytecompositions described herein are solid compositions, they can serve asseparators, particularly when they are in the form of a film.

In some embodiments, the solid electrolyte compositions serve aselectrolytes between anodes and cathodes in alkali ion batteries thatrely on intercalation of the alkali ion during cycling.

As described above, in some embodiments, the solid compositecompositions may be incorporated into an electrode of a battery. Theelectrolyte may be a compliant solid electrolyte as described above orany other appropriate electrolyte, including liquid electrolyte.

In some embodiments, a battery includes an electrode/electrolytebilayer, with each layer incorporating the ionically conductivesolid-state composite materials described herein.

FIG. 1A shows an example of a schematic of a cell according to certainembodiments. The cell includes a negative current collector 102, ananode 104, an electrolyte/separator 106, a cathode 108, and a positivecurrent collector 110. The negative current collector 102 and thepositive current collector 110 may be any appropriate electronicallyconductive material, such as copper, steel, gold, platinum, aluminum,and nickel. In some embodiments, the negative current collector 102 iscopper and the positive current collector 110 is aluminum. The currentcollectors may be in any appropriate form, such as a sheet, foil, amesh, or a foam. According to various embodiments, one or more of theanode 104, the cathode 108, and the electrolyte/separator 106 is asolid-state composite including an organic phase and sulfide conductoras described above. In some embodiments, two or more of the anode 104,the cathode 108, and the electrolyte 106 is solid-state compositeincluding an organic phase and sulfide conductor, as described above.

In some embodiments, a current collector is a porous body that can beembedded in the corresponding electrode. For example, it may be a mesh.Electrodes that include hydrophobic polymers may not adhere well tocurrent collectors in the form of foils; however meshes provide goodmechanical contact. In some embodiments, two composite films asdescribed herein may be pressed against a mesh current collector to forman embedded current collector in an electrode. In some embodiments, ahydrophilic polymer that provides good adhesion is used.

FIG. 1B shows an example of schematic of a lithium metal cellas-assembled according to certain embodiments of the invention. The cellas-assembled includes a negative current collector 102, anelectrolyte/separator 106, a cathode 108, and a positive currentcollector 110. Lithium metal is generated on first charge and plates onthe negative current collector 102 to form the anode. One or both of theelectrolyte 106 and the cathode 108 may be a composite material asdescribed above. In some embodiments, the cathode 108 and theelectrolyte 306 together form an electrode/electrolyte bilayer. FIG. 1Cshows an example of a schematic of a cell according to certainembodiments of the invention. The cell includes a negative currentcollector 102, an anode 104, a cathode/electrolyte bilayer 112, and apositive current collector 110. Each layer in a bilayer may include asulfidic conductor. Such a bilayer may be prepared, for example, bypreparing an electrolyte slurry and depositing it on an electrode layer.

All components of the battery can be included in or packaged in asuitable rigid or flexible container with external leads or contacts forestablishing an electrical connection to the anode and cathode, inaccordance with known techniques.

In the description above and in the claims, numerical ranges areinclusive of the end points of the range. For example, “y is a numberbetween 0 and 0.8” includes 0 and 0.8. Similarly, ranges represented bya dash are inclusive of the end points of the ranges.

1. A composite comprising: inorganic ionically conductive particles; andan organic phase comprising a polymer binder, wherein the polymer bindercomprises a first polymer modified with functional groups, thefunctional groups being between 0.1 and 5 wt. % of the first polymer. 2.The composite of claim 1, wherein the first polymer is a non-polarpolymer and the functional groups are polar groups.
 3. The composite ofclaim 1, wherein the functional groups are selected from:

where R, R₁, R₂, R₃ are independently for each occurrence selected from—CN, —H, —OH, Me⁺, —OMe⁺, optionally substituted aryl, optionallysubstituted alkoxy, optionally substituted alkyl, optionally substitutedalkenyl, and optionally substituted alkynyl; and X is independently foreach occurrence selected from —F , —Cl, —Br, and —I; and n is an integerfrom 1 to
 10. 4. The composite of claim 3, wherein the first polymer isone of styrene-butadiene-styrene (SBS), styrene-isoprene-styrene (SIS),styrene-ethylene/propylene-styrene (SEPS),styrene-ethylene/butylene-styrene (SEBS), styrene butadiene rubber(SBR), ethylene propylene diene monomer (EPDM) rubber, polybutadiene(PBD), polyethylene (PE), polypropylene (PP), and polystyrene (PS). 5.The composite of claim 1, wherein the polymer binder comprises SEBSmodified with maleic anhydride (SEBS-gMA).
 6. The composite of claim 5,wherein the polymer binder comprises a mixture of unmodified SEBS andSEB-gMA.
 7. The composite of claim 1, wherein the polymer bindercomprises SEBS modified with furfurylamine (SEBS-gFA).
 8. The compositeof claim 1, wherein the polymer binder comprises a mixture of the firstpolymer modified with functional groups and an unmodified first polymer.9. The composite of claim 1, wherein the inorganic ionically conductiveparticles are argyrodites.
 10. The composite of claim 1, wherein theinorganic ionically conductive particles are sulfide glass particles.11. The composition of claim 1, wherein the composite has an elongationat break of at least 10%.
 12. A slurry comprising: a solvent; a polymerbinder dissolved in the solvent, the polymer binder comprises a firstpolymer modified with functional groups, the functional groups beingbetween 0.1 and 5 wt. % of the first polymer; and ionically conductivesulfidic particles suspended in the solvent.
 13. The slurry of claim 12,wherein the solvent has a polarity index of less than 3.5.
 14. Theslurry of claim 12, wherein the solvent is halogenated and has apolarity index of higher than 3.5.
 15. The slurry of claim 12, whereinthe first polymer is a non-polar polymer and the functional groups arepolar groups.
 16. The slurry of claim 15, wherein the functional groupsare selected from:

where R, R₁, R₂, R3 are independently for each occurrence selected from—CN, —H, —OH, Me⁺, —OMe⁺, optionally substituted aryl, optionallysubstituted alkoxy, optionally substituted alkyl, optionally substitutedalkenyl, and optionally substituted alkynyl; and X is independently foreach occurrence selected from —F, —Cl, —Br, and —I; and n is an integerfrom 1 to
 10. 17. The slurry of claim 12, wherein the first polymer isone of styrene-butadiene-styrene (SBS), styrene-isoprene-styrene (SIS),styrene-ethylene/propylene-styrene (SEPS),styrene-ethylene/butylene-styrene (SEBS), styrene butadiene rubber(SBR), ethylene propylene diene monomer (EPDM) rubber, polybutadiene(PBD), polyethylene (PE), polypropylene (PP), and polystyrene (PS). 18.The slurry of claim 12, wherein the polymer binder comprises SEBSmodified with maleic anhydride (SEBS-gMA).
 19. The slurry of claim 12,wherein the polymer binder comprises SEBS modified with furfurylamine(SEBS-gFA).
 20. The slurry of claim 12, wherein the polymer bindercomprises a mixture of the first polymer modified with functional groupsand an unmodified first polymer.
 21. The slurry of claim 12, wherein thesolvent is at least 50% wt of the slurry.
 22. A composite comprising:inorganic ionically conductive particles; and an organic phasecomprising a polymer binder, wherein the polymer binder comprises afirst polymer modified with functional groups, the functional groupsbeing between 0.1 and 50 wt. % of the first polymer.
 23. The compositeof claim 22, wherein the functional groups are between 5 and 50 wt. % ofthe first polymer.
 24. The composite of claim 22, wherein the firstpolymer unmodified is insoluble in solvents having polarity indexesbelow 4.5.
 25. The composite of claim 24, wherein the first polymermodified is soluble in the solvents having polarity indexes below 4.5.26. The composite claim 22, wherein the first polymer comprisespolyvinylidene fluoride (PVDF).
 27. The composite of claim 26, whereinthe polymer binder comprises PVDF modified with styrene.
 28. Thecomposition of claim 22, wherein the inorganic ionically conductiveparticles comprise argyrodite particles.